About this trial
This study aims to inform clinical decision-making by thoroughly examining the outcomes of different treatment approaches for lateral quarter clavicle fractures and acromioclavicular dislocations. By evaluating the safety and efficacy of Knotless AC TightRope® repair devices and comparing short- and long-term results with other fixation techniques, the investigators hope to contribute to the improvement of treatment protocols for these common shoulder injuries. This research could significantly impact patients' quality of life by enabling optimal recovery and restoration of shoulder function.
Eligibility criteria
Qualifiers
Patients presenting with a fracture of the lateral quarter of the clavicle or a severe acromioclavicular disjunction (Rockwood stages III-V) confirmed by radiological examination
Patients who have given their consent to participate in the observational study after being informed by the surgeon
Disqualifiers
Minor patients;
Subjects who are legally protected adults, under guardianship or trusteeship;
Infection;
Pregnant or breastfeeding women.
Trial design
Treatments tested in this trial
- endobutton under fluoroscopic control (Knotless AC TightRope®)
Treatment groups
Sponsors and collaborators
BOUCHRA BENKESSOU
Lead sponsor
Clinique du Trocadéro
Sponsor institution